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_aEG-GiCUC _beng _cEG-GiCUC |
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| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.10.04.M.Sc.2010.Do.F | ||
| 100 | 0 | _aDoaa Mohammed Taher Abdelmohsen | |
| 245 | 1 | 0 |
_aFrequency of hemochromatosis (HFE ) gene mutations among B - thalassaemic patients with iron overload / _cDoaa Mohammed Taher Abdelmohsen ; Supervised Magdy Ahmed Elsayed Ghoniem , Eman Moawad Mohammed Gouda , Nermeen Ahmed Eldesoukey |
| 246 | 1 | 5 | _aدراسة معدل الطفرات فى جين الهيموكروماتوزس فى مرضى الثلاثيما المعرضين لزيادة عنصر الحديد |
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_aCairo : _bDoaa Mohammed Taher Abdelmohsen , _c2010 |
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_a126Leaves : _bcharts ; _c30cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Veterinary Medicine - Department of Biochemistry and Chemistry of Nutrition | ||
| 520 | _aÝ- thalassemia one of the most severe form of thalassemia is caused by defective globin production that causes anemia and also it results in iron overload which is the major cause of Ý- thalassemia mortality worldwide . Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron intake and progressive storage and is related to mutations in the HFE gene | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aHemochromatosis (HFE ) gene | |
| 653 | 4 | _aHereditary hemochromatosis (HH ) | |
| 653 | 4 | _aÝ- thalassemia | |
| 700 | 0 |
_aEman Moawad Mohammed Gouda , _eSupervisor |
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| 700 | 0 |
_aMagdy Ahmed Elsayed Ghoniem , _eSupervisor |
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| 700 | 0 |
_aNermeen Ahmed Eldesoukey , _eSupervisor |
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